Selective hydrogenation of 5-HMF to 2,5-DMF over a magnetically recoverable non-noble metal catalyst

• Published in: Green chemistry : an international journal and green chemistry resource : GC 2019, Vol.21 (23), p.639-646
• Main Authors: Solanki, Bhanupratap Singh, Rode, Chandrashekhar V
• Format: Article
• Language: English
• Subjects: Acidity; Ammonia; Bimetals; Catalysts; Copper; Furfural; Green chemistry; Hydrogenation; Hydrogenolysis; Hydroxymethylfurfural; Iron; Noble metals; Pyridines; Selectivity; X ray photoelectron spectroscopy
• ISSN: 1463-9262; 1463-9270
• DOI: 10.1039/c9gc03091c

A non-noble bimetallic catalyst Cu-Fe (1 : 2) was magnetically recoverable, highly selective and efficient for 5-(hydroxymethyl) furfural (5-HMF) hydrogenation to 2,5-dimethyl furan (DMF). The structure-activity correlation was established by characterising the prepared catalyst by XRD, XPS, TEM, ESEM, BET surface area, N 2 -adsorption, NH 3 -TPD, pyridine-IR and H 2 -TPR measurements. The high catalytic efficiency was attributed to the oxophilic nature and Lewis acidity of Fe, whereas the selectivity towards DMF was attributed to the Brønsted acidity of CuO and its affinity towards the C-O bond which was further confirmed by NH 3 -TPD and Py-IR analyses. XPS and XRD revealed the presence of Cu/CuFe 2 O 4 species which catalyzed the hydrogenolysis pathway. TEM and SEM images evidenced the presence of a Cu-Fe nanomorph in which Cu/CuFe 2 O 4 was present. The size of the Cu-Fe nanomorph was found to be between 15.4-17.6 nm. Under the optimised reaction conditions, the highest conversion of 97% and selectivity of 93% were achieved. A non-noble bimetallic catalyst Cu-Fe (1 : 2) was magnetically recoverable, highly selective and efficient for 5-(hydroxymethyl) furfural (5-HMF) hydrogenation to 2,5-dimethyl furan (DMF).